Blum Jennifer, Sheldon Wendy R, Ngoc Nguyen Thi Nhu, Winikoff Beverly, Nga Nguyen Thi Bach, Martin Roxanne, Van Thanh Le, Blumenthal Paul D
Gynuity Health Projects, New York, NY.
Gynuity Health Projects, New York, NY.
Contraception. 2016 Aug;94(2):115-21. doi: 10.1016/j.contraception.2016.04.001. Epub 2016 Apr 8.
To evaluate the accuracy, feasibility and acceptability of two urine pregnancy tests in assessing abortion outcomes at three time points after mifepristone administration.
This randomized trial enrolled women seeking early medical abortion at two hospitals in Vietnam. Investigators randomly allocated participants to at-home administration of a multilevel urine pregnancy test (MLPT) or a high sensitivity urine pregnancy test (HSPT) to assess their abortion outcomes. A baseline test was administered on the same day as mifepristone. Participants performed and interpreted results of pregnancy tests taken 3, 7 and 14days after mifepristone. Ultrasound exam determined continuing pregnancy.
Six hundred women enrolled, and 300 received each test. A percentage of 97.4 (584) had follow-up, of whom 13 women had continuing pregnancies. The specificity of MLPT at detecting absence of continuing pregnancy was 63.9%, 90.4% and 97.1% at study day 3, 7 and 14. The specificity of HSPT was 6.0%, 19.8% and 62.2%, respectively. The positive predictive value (PPV) of MLPT at detecting continuing pregnancy was 6.4% at day 3 and rose to 46.7% at day 14. In contrast, the PPV for HSPT was 2.2% at day 3 and rose to 6.5% at day 14. At all three time points, the sensitivity and negative predictive values for both tests were 100.0%. Most women found their assigned tests easy to use and would prefer future home follow-up with a pregnancy test.
The MLPT enables women to assess their abortion outcomes more reliably than with HSPT. With MLPT, women can know their outcomes as early as 3 days after mifepristone.
Medical abortion service delivery with an MLPT to obtain a baseline (preabortion) human chorionic gonadotropin (hCG) estimate and a second follow-up MLPT 1 to 2 weeks later can establish whether there has been a drop in hCG, signifying absence of a continuing pregnancy. Used this way, MLPTs can enable women to assess their abortion status outside of a clinic setting and without serum hCG testing and/or ultrasound.
评估两种尿液妊娠试验在米非司酮给药后三个时间点评估流产结局的准确性、可行性和可接受性。
这项随机试验纳入了在越南两家医院寻求早期药物流产的女性。研究人员将参与者随机分配至在家自行使用多级尿液妊娠试验(MLPT)或高灵敏度尿液妊娠试验(HSPT)来评估其流产结局。在服用米非司酮的同一天进行基线检测。参与者在服用米非司酮后3天、7天和14天进行并解读妊娠试验结果。超声检查确定是否持续妊娠。
600名女性入组,每种试验各300人接受。97.4%(584人)进行了随访,其中13名女性持续妊娠。MLPT在研究第3天、第7天和第14天检测无持续妊娠的特异性分别为63.9%、90.4%和97.1%。HSPT的特异性分别为6.0%、19.8%和62.2%。MLPT在第3天检测持续妊娠的阳性预测值(PPV)为6.4%,在第14天升至46.7%。相比之下,HSPT在第3天的PPV为2.2%,在第14天升至6.5%。在所有三个时间点,两种试验的敏感性和阴性预测值均为100.0%。大多数女性发现她们所分配的试验易于使用,并更倾向于未来在家中进行妊娠试验随访。
与HSPT相比,MLPT能使女性更可靠地评估其流产结局。使用MLPT,女性在米非司酮给药后3天就能知晓其结局。
采用MLPT进行药物流产服务,以获得基线(流产前)人绒毛膜促性腺激素(hCG)估计值,并在1至2周后进行第二次随访MLPT,可确定hCG是否下降,这表明无持续妊娠。以这种方式使用,MLPT可使女性在非诊所环境中评估其流产状态,而无需进行血清hCG检测和/或超声检查。